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首页> 外文期刊>Reproduction: The official journal of the Society for the Study of Fertility >The interaction of modified histones with the bromodomain testis-specific (BRDT) gene and its mRNA level in sperm of fertile donors and subfertile men
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The interaction of modified histones with the bromodomain testis-specific (BRDT) gene and its mRNA level in sperm of fertile donors and subfertile men

机译:修饰组蛋白与可育供体和亚供精男性精子的溴结构域睾丸特异性基因(BRDT)的相互作用及其mRNA水平

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As histone modifications have been suggested to be involved in the regulation of gene expression after fertilisation, the present study aimed to analyze the interaction between the bromodomain testis-specific ( BRDT ) gene and differentially modified histones in human spermatozoa. The BRDT transcript level was studied to identify possible correlations between epigenetic changes, mRNA level and subfertility associated with impaired sperm chromatin condensation. Chromatin immunoprecipitation (ChIP) was performed with ejaculates from fertile and subfertile men using antibodies against specifically acetylated and methylated histone H3. Immunoprecipitated DNA was analysed by real-time quantitative PCR with primer pairs for BRDT . The BRDT mRNA level was screened by real-time RT-PCR. ChIP assay revealed co-localisation of acetylated and methylated histones within promoter and exon regions of the BRDT gene in fertile men. Interestingly, reduced binding of investigated modified histone modifications was observed in the BRDT promoter of subfertile patients. Different mRNA levels of BRDT have been detected in a group of infertile patients, as well as in fertile men. Enrichment of methylated histones within the BRDT promoter of fertile sperm suggests that this epigenetic mark may cause repression of BRDT after fertilisation, and may be changed in infertile patients. Our data suggest that reduced histone methylation in the promoter of BRDT may be associated with increased transcript levels in subfertile patients.
机译:由于组蛋白修饰已被提议参与受精后基因表达的调节,因此本研究旨在分析溴结构域睾丸特异性(BRDT)基因与人精子中差异修饰的组蛋白之间的相互作用。研究了BRDT转录水平,以鉴定表观遗传变化,mRNA水平和与精子染色质凝缩受损相关的亚生育力之间的可能相关性。使用针对特异乙酰化和甲基化组蛋白H3的抗体,对可育和不育男性的射精进行染色质免疫沉淀(ChIP)。通过实时定量PCR和引物对对BRDT进行免疫沉淀DNA分析。通过实时RT-PCR筛选BRDT mRNA水平。 ChIP分析显示,在可育男性中,乙酰化和甲基化组蛋白在BRDT基因的启动子和外显子区域内共定位。有趣的是,在亚生育力患者的BRDT启动子中观察到研究的修饰的组蛋白修饰的结合减少。已在一组不育患者以及可育男性中检测到不同的BRDT mRNA水平。可育精子的BRDT启动子内甲基化组蛋白的富集表明,这种表观遗传标记可能会导致受精后BRDT的抑制,并且可能在不育患者中发生改变。我们的数据表明,BRDT启动子中组蛋白甲基化的减少可能与亚生育患者的转录水平升高有关。

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